Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17404153
rs17404153
5 3 132444356 intron variant G/T snv 0.10 0.800 1.000 2 2013 2018
dbSNP: rs17345563
rs17345563
1 3 132490359 intron variant A/G snv 9.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs78946096
rs78946096
3 3 132469319 intron variant A/G snv 3.8E-02 0.700 1.000 1 2018 2018